Cargando…

Cell division machinery drives cell-specific gene activation during bacterial differentiation

When faced with starvation, the bacterium Bacillus subtilis transforms itself into a dormant cell type called a “spore”. Sporulation initiates with an asymmetric division event, which requires the relocation of the core divisome components FtsA and FtsZ, after which the sigma factor σ(F) is exclusiv...

Descripción completa

Detalles Bibliográficos
Autores principales: Chareyre, Sylvia, Li, Xuesong, Anjuwon-Foster, Brandon R., Clifford, Sarah, Brogan, Anna, Su, Yijun, Shroff, Hari, Ramamurthi, Kumaran S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10542145/
https://www.ncbi.nlm.nih.gov/pubmed/37790399
http://dx.doi.org/10.1101/2023.08.10.552768
_version_ 1785114031639494656
author Chareyre, Sylvia
Li, Xuesong
Anjuwon-Foster, Brandon R.
Clifford, Sarah
Brogan, Anna
Su, Yijun
Shroff, Hari
Ramamurthi, Kumaran S.
author_facet Chareyre, Sylvia
Li, Xuesong
Anjuwon-Foster, Brandon R.
Clifford, Sarah
Brogan, Anna
Su, Yijun
Shroff, Hari
Ramamurthi, Kumaran S.
author_sort Chareyre, Sylvia
collection PubMed
description When faced with starvation, the bacterium Bacillus subtilis transforms itself into a dormant cell type called a “spore”. Sporulation initiates with an asymmetric division event, which requires the relocation of the core divisome components FtsA and FtsZ, after which the sigma factor σ(F) is exclusively activated in the smaller daughter cell. Compartment specific activation of σ(F) requires the SpoIIE phosphatase, which displays a biased localization on one side of the asymmetric division septum and associates with the structural protein DivIVA, but the mechanism by which this preferential localization is achieved is unclear. Here, we isolated a variant of DivIVA that indiscriminately activates σ(F) in both daughter cells due to promiscuous localization of SpoIIE, which was corrected by overproduction of FtsA and FtsZ. We propose that a unique feature of the sporulation septum, defined by the cell division machinery, drives the asymmetric localization of DivIVA and SpoIIE to trigger the initiation of the sporulation program.
format Online
Article
Text
id pubmed-10542145
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Cold Spring Harbor Laboratory
record_format MEDLINE/PubMed
spelling pubmed-105421452023-10-03 Cell division machinery drives cell-specific gene activation during bacterial differentiation Chareyre, Sylvia Li, Xuesong Anjuwon-Foster, Brandon R. Clifford, Sarah Brogan, Anna Su, Yijun Shroff, Hari Ramamurthi, Kumaran S. bioRxiv Article When faced with starvation, the bacterium Bacillus subtilis transforms itself into a dormant cell type called a “spore”. Sporulation initiates with an asymmetric division event, which requires the relocation of the core divisome components FtsA and FtsZ, after which the sigma factor σ(F) is exclusively activated in the smaller daughter cell. Compartment specific activation of σ(F) requires the SpoIIE phosphatase, which displays a biased localization on one side of the asymmetric division septum and associates with the structural protein DivIVA, but the mechanism by which this preferential localization is achieved is unclear. Here, we isolated a variant of DivIVA that indiscriminately activates σ(F) in both daughter cells due to promiscuous localization of SpoIIE, which was corrected by overproduction of FtsA and FtsZ. We propose that a unique feature of the sporulation septum, defined by the cell division machinery, drives the asymmetric localization of DivIVA and SpoIIE to trigger the initiation of the sporulation program. Cold Spring Harbor Laboratory 2023-08-10 /pmc/articles/PMC10542145/ /pubmed/37790399 http://dx.doi.org/10.1101/2023.08.10.552768 Text en https://creativecommons.org/publicdomain/zero/1.0/This article is a US Government work. It is not subject to copyright under 17 USC 105 and is also made available for use under a CC0 license (https://creativecommons.org/publicdomain/zero/1.0/) .
spellingShingle Article
Chareyre, Sylvia
Li, Xuesong
Anjuwon-Foster, Brandon R.
Clifford, Sarah
Brogan, Anna
Su, Yijun
Shroff, Hari
Ramamurthi, Kumaran S.
Cell division machinery drives cell-specific gene activation during bacterial differentiation
title Cell division machinery drives cell-specific gene activation during bacterial differentiation
title_full Cell division machinery drives cell-specific gene activation during bacterial differentiation
title_fullStr Cell division machinery drives cell-specific gene activation during bacterial differentiation
title_full_unstemmed Cell division machinery drives cell-specific gene activation during bacterial differentiation
title_short Cell division machinery drives cell-specific gene activation during bacterial differentiation
title_sort cell division machinery drives cell-specific gene activation during bacterial differentiation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10542145/
https://www.ncbi.nlm.nih.gov/pubmed/37790399
http://dx.doi.org/10.1101/2023.08.10.552768
work_keys_str_mv AT chareyresylvia celldivisionmachinerydrivescellspecificgeneactivationduringbacterialdifferentiation
AT lixuesong celldivisionmachinerydrivescellspecificgeneactivationduringbacterialdifferentiation
AT anjuwonfosterbrandonr celldivisionmachinerydrivescellspecificgeneactivationduringbacterialdifferentiation
AT cliffordsarah celldivisionmachinerydrivescellspecificgeneactivationduringbacterialdifferentiation
AT brogananna celldivisionmachinerydrivescellspecificgeneactivationduringbacterialdifferentiation
AT suyijun celldivisionmachinerydrivescellspecificgeneactivationduringbacterialdifferentiation
AT shroffhari celldivisionmachinerydrivescellspecificgeneactivationduringbacterialdifferentiation
AT ramamurthikumarans celldivisionmachinerydrivescellspecificgeneactivationduringbacterialdifferentiation